CTNNA3 (catenin alpha 3)

2007-06-01   Dessen P  

Identity

HGNC
LOCATION
10q21.3
LOCUSID
ALIAS
ARVD13,VR22
FUSION GENES

Other Information

Locus ID:

NCBI: 29119
MIM: 607667
HGNC: 2511
Ensembl: ENSG00000183230

Variants:

dbSNP: 29119
ClinVar: 29119
TCGA: ENSG00000183230
COSMIC: CTNNA3

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000183230ENST00000330298Q5SW23
ENSG00000183230ENST00000433211Q9UI47
ENSG00000183230ENST00000494580V9GYW4
ENSG00000183230ENST00000545309F2Z2R0

Expression (GTEx)

0
5
10
15
20
25
30

Pathways

PathwaySourceExternal ID
Adherens junctionKEGGko04520
Leukocyte transendothelial migrationKEGGko04670
Endometrial cancerKEGGko05213
Adherens junctionKEGGhsa04520
Leukocyte transendothelial migrationKEGGhsa04670
Pathways in cancerKEGGhsa05200
Endometrial cancerKEGGhsa05213
Arrhythmogenic right ventricular cardiomyopathy (ARVC)KEGGko05412
Arrhythmogenic right ventricular cardiomyopathy (ARVC)KEGGhsa05412
Bacterial invasion of epithelial cellsKEGGko05100
Bacterial invasion of epithelial cellsKEGGhsa05100
Hippo signaling pathwayKEGGhsa04390
Hippo signaling pathwayKEGGko04390

Protein levels (Protein atlas)

Not detected
Low
Medium
High

PharmGKB

Entity IDNameTypeEvidenceAssociationPKPDPMIDs
PA447321Depressive Disorder, MajorDiseaseClinicalAnnotationassociatedPD
PA452229antidepressantsChemicalClinicalAnnotationassociatedPD

References

Pubmed IDYearTitleCitations
371266832023Proteomics and phosphoproteomics of failing human left ventricle identifies dilated cardiomyopathy-associated phosphorylation of CTNNA3.4
371266832023Proteomics and phosphoproteomics of failing human left ventricle identifies dilated cardiomyopathy-associated phosphorylation of CTNNA3.4
347176012021CTNNA3 genetic polymorphism may be a new genetic signal of type 2 diabetes in the Chinese Han population: a case control study.1
347176012021CTNNA3 genetic polymorphism may be a new genetic signal of type 2 diabetes in the Chinese Han population: a case control study.1
286996312017Co-inheritance of mutations associated with arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathy.9
288016522017Assessment of Three New Loci from Genome-wide Association Study in Essential Tremor in Chinese population.5
286996312017Co-inheritance of mutations associated with arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathy.9
288016522017Assessment of Three New Loci from Genome-wide Association Study in Essential Tremor in Chinese population.5
268825632016CTNNA3 is a tumor suppressor in hepatocellular carcinomas and is inhibited by miR-425.24
270911892016Genome-wide association study of antidepressant response: involvement of the inorganic cation transmembrane transporter activity pathway.11
272723922016Polymorphisms of CHAT but not TFAM or VR22 are Associated with Alzheimer Disease Risk.2
277656352016Molecular Analysis of Hybrid Neurofibroma/Schwannoma Identifies Common Monosomy 22 and α-T-Catenin/CTNNA3 as a Novel Candidate Tumor Suppressor.11
277978062016Genome-wide association study in essential tremor identifies three new loci.35
268825632016CTNNA3 is a tumor suppressor in hepatocellular carcinomas and is inhibited by miR-425.24
270911892016Genome-wide association study of antidepressant response: involvement of the inorganic cation transmembrane transporter activity pathway.11

Citation

Dessen P

CTNNA3 (catenin alpha 3)

Atlas Genet Cytogenet Oncol Haematol. 2007-06-01

Online version: http://atlasgeneticsoncology.org/gene/47565/ctnna3-(catenin-alpha-3)